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Home Healthcare

AllImplants & Prosthetics(226)Monitoring Devices(265)Diagnostic Equipment(820)Home Healthcare(225)Contact Lenses & Vision(17)Surgical Equipment(893)

225 recalls

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Max Mobility
Critical RiskFDA Device

Max Mobility Smart Drive SpeedControl Dials Recalled for Loss of Control Risk

  • Sold in 52 states
  • Sold at Authorized Wheelchair Dealers, Medical Equipment Suppliers +1 more
  • 49,636 units affected
Recalled
Added
Fresenius Medical Care
Medium RiskFDA Device

Fresenius Medical Care Holdings, Inc.: Stay Safe Cap Recalled for Updated Safety Warnings and Contraindications

  • Distributed nationwide
  • Sold at authorized medical distributors, healthcare providers
  • 18,236,160 units affected
Recalled
Added
SleepNet Corporation: CPAP and Nasal Masks Recalled for Updated Magnetic Interference Warnings
Critical RiskFDA Device

SleepNet Corporation: CPAP and Nasal Masks Recalled for Updated Magnetic Interference Warnings

  • Distributed nationwide
  • Sold at Authorized medical equipment distributors
  • 45,972 units affected
Recalled
Added
Medtronic MiniMed
Medium RiskFDA Device

Medtronic InPen Smart Insulin Pens Recalled for Assembly Defect

  • Sold in 41 states
  • Sold at Authorized medical distributors
Recalled
Added
Medium RiskFDA Device

MediHoney Wound Dressings Recalled for Packaging Failure and Sterility Risk

  • Sold in 13 states
  • Sold at CVS, authorized distributors +1 more
  • 107,549 units affected
Recalled
Added
Medline Industries
Medium RiskFDA Device

Curad Touch-Free and Quick-Strip Bandages Recalled for Sterility Risk

  • Distributed nationwide
  • Sold at Retail Stores, Medical Suppliers
  • 26,155,726 units affected
Recalled
Added
mo-Vis BVBA
Medium RiskFDA Device

mo-Vis BVBA: Scoot Control R-net Recalled for Sticking Throttle and Unwanted Movement

  • Sold in Tennessee, Texas
  • Sold at Authorized wheelchair dealers, Medical equipment distributors
Recalled
Added
Sol-Millennium Medical
Medium RiskFDA Device

Sol-Millennium Medical Inc.: Various Syringes and Tip Caps Recalled for Unauthorized Design Changes

  • Distributed nationwide
  • Sold at Medline, Henry Schein +1 more
Recalled
Added
Unomedical A/S
Medium RiskFDA Device

Unomedical A/S: Neria Soft Infusion Sets Recalled for Incorrect Instructions for Use

  • Sold in Florida
  • Sold at Osted
  • 10,770 units affected
Recalled
Added
DAYE (ANNE'S DAY LTD)
Medium RiskFDA Device

Daye Tampons and Product Bundles Recalled for Lack of FDA Clearance

  • Distributed nationwide
  • Sold at Direct distribution, Retail packs
Recalled
Added
ICU Medical
Medium RiskFDA Device

Smiths Medical CADD Medication Cassette Reservoirs Recalled for Leakage Risk

  • Distributed nationwide
  • Sold at Hospitals, Infusion Centers +1 more
  • 1,799,616 units affected
Recalled
Added
ETAC A/S
Medium RiskFDA Device

Molift Mover Hoists and Sling Bars Recalled for Lifting Bar Joint Defect

  • Sold in Pennsylvania
  • Sold at Authorized Medical Equipment Distributors
Recalled
Added
Smiths Medical ASD
Critical RiskFDA Device

CADD-Solis Infusion Pumps Recalled for False Alarms and Infusion Interruptions

  • Distributed nationwide
  • Sold at Authorized medical device distributors, Hospitals +1 more
  • Serious patient injury or death possible due to interruption of therapy; specific counts not provided.
Recalled
Added
Philips Respironics
Critical RiskFDA Device

Philips Respironics, Inc.: Trilogy and Garbin EVO Ventilators Recalled for Sudden Loss of Ventilation

  • Distributed nationwide
  • Sold at Authorized Medical Device Distributors, Specialty Retailers +1 more
  • 146,523 units affected
Recalled
Added
Fresenius Medical Care
Critical RiskFDA Device

Fresenius Medical Care Holdings, Inc.: stay-safe Catheter Extensions and Adapters Recalled for Tubing Contamination

  • Distributed nationwide
  • Sold at Fresenius Medical Care Holdings, Inc., Medical distributors
  • NDL PCBAs contamination
Recalled
Added
Boston Scientific
High RiskFDA Device

Boston Scientific Corporation: EndoVive PEG Feeding Tube Kits Recalled for Blocked Barb Connector

  • Distributed nationwide
  • Sold at Boston Scientific Corporation, Medical Supply Distributors
Recalled
Added
Baxter Healthcare
Critical RiskFDA Device

Welch Allyn and Breathe Technologies Life2000 Ventilators Recalled for Battery Failure

  • Distributed nationwide
  • Sold at authorized healthcare dealers, medical equipment suppliers
Recalled
Added
Baxter Healthcare
Medium RiskFDA Device

Baxter MiniCap PD Transfer Sets Recalled for Connector Separation Risk

  • Distributed nationwide
  • Sold at Baxter Healthcare Corporation, Medical distributors
  • An increase in complaints related to connector separation was reported; specific injury counts not provided.
Recalled
Added
Applied Medical Technology
Medium RiskFDA Device

Applied Medical Technology NutraGlide Nasal Feeding Tubes Recalled for Occlusion

  • Sold in 4 states
  • Sold at Hospitals, Medical Supply Distributors +1 more
Recalled
Added
Fresenius Kabi USA
Critical RiskFDA Device

Fresenius Kabi USA, LLC: Ivenix Infusion System Recalled Due to Potential Fluid Valve Failure

  • Sold in 5 states
  • Sold at authorized healthcare distributors, hospitals
Recalled
Added
Visonic Recalls Amber Personal Emergency Response System Kits Due to Remote Pendant Battery Signal Failure
Medium RiskCPSC

Visonic Recalls Amber Personal Emergency Response System Kits Due to Remote Pendant Battery Signal Failure

  • Distributed nationwide
  • Sold at Visonic distributors and professional alarm installation firms nationwide from January 2008 through August 2013 for between $220 and $240 for the kits.
  • The firm received one report of a pendant that failed to operate due to a low battery undetected by the base station in Common Area Mode. No injuries have been reported.
Recalled
Added
Linear Recalls Personal Emergency Reporting System Transmitters Due to Battery Signal Failure
Medium RiskCPSC

Linear Recalls Personal Emergency Reporting System Transmitters Due to Battery Signal Failure

  • Distributed nationwide
  • Sold at Independent PERS distributors and dealers nationwide from June 2013 through August 2013 for about $45.
  • Linear received one report of a transmitter that failed to operate. No injuries have been reported.
Recalled
Added
Visonic Amber Personal Emergency Response Kits Recalled Due to Failure to Signal Emergency Assistance
Medium RiskCPSC

Visonic Amber Personal Emergency Response Kits Recalled Due to Failure to Signal Emergency Assistance

  • Distributed nationwide
  • Sold at Visonic distributors and professional alarm installation firms nationwide from April 2012 through April 2013 for between $220 and $240 for the kits.
  • The firm has not received any reports of incidents or injuries related to this issue.
Recalled
Added
Adult Portable Bed Handles Recalled by Bed Handles Inc. Due to Entrapment and Strangulation Hazards; Three Deaths Reported
Medium RiskCPSC

Adult Portable Bed Handles Recalled by Bed Handles Inc. Due to Entrapment and Strangulation Hazards; Three Deaths Reported

  • Distributed nationwide
  • Sold at Home health care stores, drug stores and medical equipment stores nationwide and in home and health care catalogs from January 1994 through December 2007 for about $100.
  • Three women died after becoming entrapped between the mattress and the bed handles. They include an elderly woman, age unknown, who died in an Edina, Minn. assisted living facility; a 41-year-old disabled woman who died in a Renton, Wash. adult family home; and an 81-year-old woman who died in a Vancouver, Wash. managed care facility.
Recalled
Added